Selective cleavage of protonated penetratin and its substitutes under low-energy collision-induced dissociation condition

被引:7
作者
Peng, Juan [1 ]
Zu, Lily [1 ]
Fang, Weihai [1 ]
Huang, Lingyun [2 ]
Wang, Yaru [1 ]
He, Dacheng [2 ]
机构
[1] Beijing Normal Univ, Dept Chem, Beijing 100875, Peoples R China
[2] Beijing Normal Univ, Key Lab Cell Proliferat & Regulat, Minist Educ, Beijing 100875, Peoples R China
来源
JOURNAL OF MASS SPECTROMETRY | 2010年 / 45卷 / 06期
基金
中国国家自然科学基金;
关键词
penetratin; substitutes; selective cleavage; collision-induced dissociation; ESI-Q-TOF MS/MS; MAIN FRAGMENTATION PATHWAYS; GAS-PHASE FRAGMENTATION; TANDEM MASS-SPECTRA; GLN-GLY CLEAVAGE; AB-INITIO; ION CHEMISTRY; AMINO-ACIDS; AMIDE BOND; PEPTIDES; OLIGOPEPTIDES;
D O I
10.1002/jms.1748
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An understanding of the dissociation of penetratin is important for improving its metabolic stability and cargo-delivery efficiency. In this study, we describe the selective cleavage of the K15-K16 amide bond of penetratin under the low-energy collision-induced dissociation condition in mass spectrometry. A variety of penetratin substitutes have been studied in which key basic amino acids have been substituted within the sequence. The calculated structure indicates that an a-helix structure prevents the fragmentation of the central peptide domain and the side chain of lysine is involved in the proton translocation process. Copyright (C) 2010 John Wiley & Sons, Ltd.
引用
收藏
页码:627 / 634
页数:8
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